Surface Modification of Polyimide Aerogel by Thermoplastic Polyurethane for Enhanced Mechanical Strength and Thermal Insulation Performance.

Polyimide (PI) aerogel is a good thermal insulation material with the highest temperature resistance in practical application. But the mechanical strength of PI aerogels prepared by freeze-drying or thermoimide methods is weak. In this research, TPU was selected as an aging solution to solve the problem of the low mechanical strength of PI aerogel prepared by the freeze-drying method. Previous work has certified that the coupling of PI and thermoplastic polyurethane (TPU) can enhance the mechanical strength of PI aerogel to a certain extent due to the flexibility of TPU. But excessive TPU will change the PI structure in the cross-linking process and decrease the mechanical strength of the aerogel. Thus, a new kind of PI gel modification method was provided by using TPU as an aging solution, and the mechanical strength of PI aerogel is improved to 3.06 MPa. Furthermore, the shrinkage, specific surface area, waterproof angle, and thermal conductivity all show good performance, thus enabling PI aerogel to be used in many aspects. Specially, the method is simple and can be used to prepare some other high-strength aerogels.

Carboxymethyl cellulose/polyvinyl alcohol composite aerogel supported beta molecular sieve for CH4 adsorption and storage.

Biomass aerogel is attractive in various applications due to their renewable, biodegradable and eco-friendly advantages. Herein, a novel beta molecular sieve/carboxymethyl cellulose/polyvinyl alcohol composite aerogel (beta/CP) is prepared by direct mixing and directional freeze-drying as an efficient gas adsorbent with hierarchical porosity. The beta molecular sieve is uniformly dispersed in the three-dimensional skeleton of the aerogel. By adjusting the loading mass of the beta molecular sieve to constitute a reasonable porosity and pore size distribution, the synergistic effect between pore structures of different scales improves the adsorption performance. The experiment results of beta/CP-4 show that the CH4 adsorption capacity can reach 60.33 cm3/g at 298 K and 100 bar, which is almost the same as that of the pure beta molecular sieve (62.09 cm3/g). The strong interaction between the aerogel and it prevents the molecular sieve agglomeration, improves the pore utilization, and also reduces the cost of using molecular sieve adsorbent. The above results indicate that the composite has good potential for application in the field of CH4 storage.

A multifunctional PAN/PVP nanofiber sponge wound dressing loaded with ZIF-8-derived carbon nanoparticles with adjustable wetness for rapid wound disinfection and exudate management.

Rapid and safe disinfection and exudate management are two major challenges in infected wound care. Therefore, in this work, we developed a novel wound dressing via encapsulating ZIF-8-derived carbon nanoparticles in a hydrophilic nanofiber sponge to address severe wound infection and heavy exudate problems. The dressing can effectively kill bacteria through chemo-photothermal synergistic therapy. Meanwhile, the hydrophilic nanofiber sponge can quickly absorb wound exudate around the wound and accelerate the evaporation rate of liquid through the photothermal effect and its own structure; therefore, it is possible to remove excess liquid and regulate its wetness. In this way, it prevents the problem of wound overhydration often caused by hydrophilic dressings. In our experiment, the dressing showed good antibacterial performance and biocompatibility in vitro and could effectively control wound infection, absorb wound exudate and promote skin wound healing in vivo. Its good therapeutic effect is not only due to effective infection control and wound exudate management, but also because the structure of nanofibers similar to an extracellular matrix provides basic physical support and structural  signals conducive to skin tissue regeneration.

Sodium Alginate-Based Carbon Aerogel-Supported ZIF-8-Derived Porous Carbon as an Effective Adsorbent for Methane Gas.

Adsorption natural gas (ANG) is a technology in which natural gas is stored on the surface of porous materials at relatively low pressures, which are promising candidates for adsorption of natural gas. Adsorbent materials with a large surface area and porous structure plays a significant role in the ANG technology, which holds promise in increasing the storage density for natural gas while decreasing the operating pressure. Here, we demonstrate a facile synthetic method for rational construction of a sodium alginate (SA)/ZIF-8 composite carbon aerogel (AZSCA) by incorporating ZIF-8 particles into SA aerogel through a directional freeze-drying method followed by the carbonization process. The structure characterization shows that AZSCA has a hierarchical porous structure, in which the micropores originated from MOF while the mesopores are derived from the three-dimensional network of the aerogel. The experimental results show that AZSCA achieved high methane adsorption of 181 cm3·g-1 at 65 bar and 298 K, along with higher isosteric heat of adsorption (Qst) throughout the adsorption range. Thus, the combination of MOF powders with aerogel can find potential applications in other gas adsorption.

A single dual-targeting fluorescent probe enables exploration of the correlation between the plasma membrane and lysosomes.

The interactions between organelles can maintain normal cell activity. Lysosomes, as waste disposal systems of cells, have many important interactions with the plasma membrane, especially in the repair of cracked plasma membrane. Unfortunately, a way to study the relationship between them synchronously is still lacking. Therefore, in this work, we constructed a dual-targeting probe (Mem-Lyso) to simultaneously visualize the plasma membrane and lysosomes for the first time. Taking advantage of dual-targeting, the probe Mem-Lyso could successfully track and analyze the dynamic changes of the plasma membrane and lysosomes in different bioprocesses. The experimental results demonstrated that, compared to the normal status, there was obvious fusion between the plasma membrane and lysosomes in the apoptosis process. Furthermore, because of the sensitivity to polarity, Mem-Lyso could label the plasma membrane and lysosomes with red and yellow colors in cells, respectively. Moreover, the skeleton and gastrointestinal wall of zebrafish were visualized by dual-color imaging, respectively. More importantly, the dual-targeting property endowed Mem-Lyso with the ability to spatially distinguish the cholesterol (CL) content in the plasma membrane, which provided a potential detection tool for biological research and diagnosis of related diseases.

Preparation and Properties of the Urea-Formaldehyde Res-In/Reactive Halloysite Nanocomposites Adhesive with Low-Formaldehyde Emission and Good Water Resistance.

Low-cost urea formaldehyde resin (UF)/reactive halloysite nanotubes (HNTs) nanocomposite adhesive was prepared successfully via in situ polymerization. The HNTs were modified to improve its compatibility with polymer. The XRD and FTIR results showed that physical and chemical interaction between the HNTs and polymer resin influenced the structure of UF owing to the functional groups on the HNTs. It is found from SEM images that the modified HNTs could be dispersed uniformly in the resin and the nanocomposite particles were spherical. The performance experiment confirmed that thermal stability of nanocomposite increased largely, formaldehyde emission of UF wood adhesive reduced 62%, and water resistance of UF wood adhesive improved by 84%. Meanwhile, the content of HNTs on the nanocomposites could be up to 60 wt %. The mechanism of the nanocomposites based on the reactive HNTs was proposed. The approach of the preparation could supply an idea to prepare other polymer/clay nanocomposites.

Z-scheme polyimide/tungsten trioxide aerogel photocatalyst for enhanced photocatalytic CO2reduction under visible light.

Developing highly efficient and stable photocatalysts is an effective method to achieve CO2photocatalytic reduction. Herein, PI/WO3aerogel photocatalyst was prepared by chemical amide reaction coupled with an ethanol supercritical drying technique. The novel aerogel photocatalysts exhibit excellent photocatalytic performance for reducing CO2into CO. In particular, PI/WO3-10 aerogel photocatalyst shows the highest yield of CO (5.72µmol g-1h-1), which is ca 11-fold higher than that of the pristine PI aerogel. The high CO2reduction activity can be attributed to the Z-scheme structure, which enhances the separation of photo-generated electron-holes, and induces H2O oxidation on WO3nanosheets and CO2reduction on PI aerogel. The photocatalytic reaction mechanism of CO2when using PI/WO3aerogel photocatalyst is proposed.

Nitrogen-doped carbon composite derived from ZIF-8/polyaniline@cellulose-derived carbon aerogel for high-performance symmetric supercapacitors.

Cellulose derived carbon aerogel (CA) with unique three-dimensional network coated with polyaniline (PANI) on its surface is used as a scaffolding framework to anchor ZIF-8. The designed ZIF-8 derived porous carbon (ZC)/PANI@CA (ZPCA) hybrid carbon composite through a facile solution immersion chemical route and subsequent carbonization process is employed as electrode for supercapacitor, which has contributed a large specific surface area, a hierarchical porous structure and reasonable N content (up to 6.27 at.%). The synthesized ZPCA electrode achieves an outstanding capacitance of 388 F g-1 at 0.5 A g-1 as well as an excellent cycling performance. More inspiringly, the symmetric supercapacitor based ZPCA achieves a high energy density of 13.4 Wh kg-1 at a power density of 250 W kg-1 using 2 M KOH aqueous solution, and an ultrahigh energy density of 81.8 Wh kg-1 at a power density of 950 W kg-1 is realized using Et4NBF4/AN electrolyte.

High-performance asymmetric supercapacitor made of NiMoO4 nanorods@Co3O4 on a cellulose-based carbon aerogel.

In this study, a new nanoporous material comprising NiMoO4 nanorods and Co3O4 nanoparticles derived from ZIF-67 supported by a cellulose-based carbon aerogel (CA) has been successfully synthesized using a two-step hydrothermal method. Due to its chemical composition, the large specific surface and the hierarchical porous structure, the NiMoO4@Co3O4/CA ternary composite yields electrodes with an enhanced specific capacitance of 436.9 C/g at a current density of 0.5 A/g and an excellent rate capability of 70.7% capacitance retention at 5.0 A/g. Moreover, an advanced asymmetric supercapacitor (ASC) is assembled using the NiMoO4@Co3O4/CA ternary composite as the positive electrode and activated carbon as the negative electrode. The ASC device exhibits a large capacitance of 125.4 F/g at 0.5 A/g, a maximum energy density of 34.1 Wh/kg at a power density of 208.8 W/kg as well as a good cyclic stability (84% after 2000 cycles), indicating its wide applicability in energy storage. Finally, our results provide a general approach to the construction of CA and MOF-based composite materials with hierarchical porous structure for potential applications in supercapacitors.

Highly efficient visible-light-induced photoactivity of carbonized polyimide aerogel for antibiotic degradation.

Various nitrogen (N)-doped carbon materials have been designed as efficient photocatalysts. For the first time, polyimide (PI) aerogels were calcined to be N-doped carbon photocatalysts at different temperatures. The structures of the carbonized polyimide aerogels (CPIs) vary with the carbonization temperature. The conductivity of the CPI increases with the improvement of calcination temperature, whereas the N content of the CPI decreases and the N state also changes. Thus, the electronic properties of the CPI are changed. The photocatalytic experiments certified that the PI aerogel calcined at 800 °C exhibited the highest photocatalytic performance. The chlortetracycline (CTC) degradation rate over CPI-800 aerogel is 2.3 times as much as that of PI aerogel due to the changed structure and properties of the CPI-800 aerogel.

Construction of Uniform Cobalt-Based Nanoshells and Its Potential for Improving Li-Ion Battery Performance.

Surface cobalt doping is an effective and economic way to improve the electrochemical performance of cathode materials. Herein, by tuning the precipitation kinetics of Co2+, we demonstrate an aqueous-based protocol to grow uniform basic cobaltous carbonate coating layer onto different substrates, and the thickness of the coating layer can be adjusted precisely in nanometer accuracy. Accordingly, by sintering the cobalt-coated LiNi0.5Mn1.5O4 cathode materials, an epitaxial cobalt-doped surface layer will be formed, which will act as a protective layer without hindering charge transfer. Consequently, improved battery performance is obtained because of the suppression of interfacial degradation.

Monolithic zirconia aerogel from polyacetylacetonatozirconium precursor and ammonia hydroxide gel initiator: formation mechanism, mechanical strength and thermal properties.

Zirconia (ZrO2) aerogels are potential candidates for use at temperatures higher than those attainable with silica aerogels. However, fabricating a robust ZrO2 aerogel with a high thermal stability is still a challenge. The extreme electronegativity of Zr makes the hydrolysis and polycondensation of zirconium precursors difficult to control, leading to poor structural integrity and unsatisfactory physical properties. In the present research, we prepared a ZrO2 aerogel by using a synthetic zirconium precursor, namely polyacetylacetonatozirconium (PAZ), and ammonia hydroxide as the gel initiator. The ammonia hydroxide catalyzes the cross-linking of PAZ via promotion of the dehydration between hydroxyls in PAZ and the acetylacetonate group in PAZ binds the zirconium ion firmly upon the addition of ammonia hydroxide to avoid a gel precipitate. A monolithic ZrO2 aerogel with a large diameter size of 4.4 cm and high optical transmittance was achieved after drying. The surface area and pore volume of the as-dried ZrO2 aerogel were as high as 630.72 m2 g-1 and 5.12 cm3 g-1, respectively. They decreased to 188.62 m2 g-1 and 0.93 cm3 g-1 after being heat-treated at 1000 °C for 2 h. The best mechanical performances of the ZrO2 aerogels showed a compressive strength of 0.21 ± 0.05 MPa and a modulus of 1.9 ± 0.3 MPa with a density of 0.161 ± 0.008 g cm-3. Both pore structures and mechanical performances varied according to the ammonia hydroxide gel initiator used. The thermal insulating properties of the ZrO2 aerogel performed better than a silica aerogel blanket with a thermal conductivity of 0.020 W (m-1 K-1).

Microbial-Phosphorus-Enabled Synthesis of Phosphide Nanocomposites for Efficient Electrocatalysts.

Transition-metal phosphides have recently been identified as low-cost and efficient electrocatalysts that are highly active for the hydrogen evolution reaction. Unfortunately, to achieve a controlled phosphidation of nonprecious metals toward a desired nanostructure of metal phosphides, the synthetic processes usually turned complicated, high-cost, and even dangerous due to the reaction chemistry related to different phosphorus sources. It becomes even more challenging when considering the integration of those active metal phosphides with the structural engineering of their conductive matrix toward a favorable architecture for optimized catalytic performance. Herein, we identified that the biomass itself could act as an effective synthetic platform for the construction of supported metal phosphides by recovering its inner phosphorus upon reacting with transition-metals ions, forming well-dispersed, highly active nanoparticles of metal phosphides incorporated in the nanoporous carbon matrix, which promised high catalytic activity in the hydrogen evolution reaction. Our synthetic protocol not only provides a simple and effective strategy for the construction of a large variety of highly active nanoparticles of metal phosphides but also envisions new perspectives on an integrated utilization of the essential ingredients, particularly phosphorus, together with the innate architecture of the existing biomass for the creation of functional nanomaterials toward sustainable energy development.

Controlled formation of uniform nanoshells of manganese oxide and their potential in lithium ion batteries.

Uniform nanoshells of manganese oxides have been successfully prepared by controlling their growth kinetics in solution. The prepared manganese oxides show promising electrochemical performance when used as an anode material in lithium ion batteries.

Sex-dependent regulation of hepatic CYP3A by growth hormone: Roles of HNF6, C/EBPα, and RXRα.

Sex-based differences in the pharmacological profiles of many drugs are due in part to the female-predominant expression of CYP3A4, which is the most important CYP isoform responsible for drug metabolism. Transcription factors trigger the sexually dimorphic expression of drug-metabolizing enzymes in response to sex-dependent growth hormone (GH) secretion. We investigated the roles of HNF6, C/EBPα, and RXRα in the regulation of human female-predominant CYP3A4, mouse female-specific CYP3A41, and rat male-specific CYP3A2 expression by GH secretion patterns using HepG2 cells, growth hormone receptor (GHR) knockout mice as well as rat models of orchiectomy and hypophysectomy. The constitutive expression of HNF6 and RXRα was GH-dependent, and GHR deficiency decreased HNF6/C/EBPα complex levels and increased HNF6/RXRα complex levels. Feminine GH secretion induced the binding of HNF6 and C/EBPα to the CYP3A4 and Cyp3a41 promoters and HNF6/C/EBPα complex levels was more efficiently compared with masculine pattern. Additionally, a greater inhibition of the binding of RXRα to the CYP3A4 and Cyp3a41 promoters and HNF6/RXRα complex levels was observed by feminine GH secretion, but less inhibition was observed by masculine pattern. The binding of HNF6, C/EBPα, and RXRα to the CYP3A2 promoter was not directly regulated by androgens. RXRα completely abolished the synergistic activation of the CYP3A4, Cyp3a41, and CYP3A2 promoters by HNF6 and C/EBPα. The results demonstrate that sex-dependent GH secretion patterns affect the expressions and interactions of HNF6, C/EBPα, and RXRα as well as their binding to CYP3A genes. RXRα mediates the sex-dependent influence of GH on CYP3A expression as an important signalling molecule.